Reduced ejection fraction
Symptom Information:
| Symptom ID: | HPO:0012664 | ||
| Synonyms: |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Abnormal echocardiogram(HPO:0003116) Reduced ejection fraction(HPO:0012664) MedDRA: |
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| Database Frequency: | 32 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ATTRV122I amyloidosis | (Orphanet:85451) |
| Alpha-mannosidosis | (Orphanet:61) |
| Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
| Arrhythmogenic right ventricular dysplasia, familial, 13 | (OMIM:615616) |
| Arrhythmogenic right ventricular dysplasia, familial, 2 | (OMIM:600996) |
| Atrial fibrillation, familial, 3 | (OMIM:607554) |
| Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
| Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
| Cardiomyopathy, dilated, 1BB | (OMIM:612877) |
| Cardiomyopathy, dilated, 1EE | (OMIM:613252) |
| Cardiomyopathy, dilated, 1FF | (OMIM:613286) |
| Cardiomyopathy, dilated, 1II | (OMIM:615184) |
| Cardiomyopathy, dilated, 1KK | (OMIM:615248) |
| Cardiomyopathy, dilated, 1U | (OMIM:613694) |
| Cardiomyopathy, dilated, 1X | (OMIM:611615) |
| Cardiomyopathy, dilated, 2B | (OMIM:614672) |
| Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
| Cardiomyopathy, familial hypertrophic, 15 | (OMIM:613255) |
| Cardiomyopathy, familial hypertrophic, 4 | (OMIM:115197) |
| Fabry disease | (Orphanet:324) |
| Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | (Orphanet:436242) |
| Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
| Heritable pulmonary arterial hypertension | (Orphanet:275777) |
| Idiopathic giant cell myocarditis | (Orphanet:329874) |
| Idiopathic pulmonary arterial hypertension | (Orphanet:275766) |
| Incessant infant ventricular tachycardia | (Orphanet:45453) |
| Microcephaly-cardiomyopathy syndrome | (Orphanet:2515) |
| Naxos disease | (Orphanet:34217) |
| Peripartum cardiomyopathy | (Orphanet:563) |
| Steinert myotonic dystrophy | (Orphanet:273) |
| Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
| X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |